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Pigmented Paravenous Chorioretinal Atrophy
An eye disease characterized by the presence of bone corpuscle pigmentation in a paravenous distribution in the ocular fundus that is caused by heterozygous mutation in the CRB1 gene on chromosome 1q31.3.
This information is for educational purposes only and is not medical advice. Always consult your healthcare provider about your specific condition and treatment.
When to seek help
Seek medical help right away if you have severe, sudden, or worsening symptoms, trouble breathing, chest pain, or any symptom that feels life-threatening. This community is for peer support and education only and is not a substitute for professional medical advice.
If you are experiencing a medical emergency, contact your local emergency services immediately.
Overview
An eye disease characterized by the presence of bone corpuscle pigmentation in a paravenous distribution in the ocular fundus that is caused by heterozygous mutation in the CRB1 gene on chromosome 1q31.3.
Resources
Join the Pigmented Paravenous Chorioretinal Atrophy community
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Posts in this community reflect personal experiences, not medical advice. Always talk to your doctor before changing your treatment.